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After each target analyte was bound to the capture probes and then to each corresponding biotinylated antibody, and finally to the versatile ECL signal probe, ECL signals were recorded using PMT or CCD as a detector.
Briefly, beads of defined spectral properties were conjugated to protein-specific capture antibodies and added along with samples (including standards of known protein concentration, control samples, and test samples) into the wells of a filter-bottom microplate, where proteins bound to the capture antibodies over the course of a 2-hour incubation.
A subsequent wash step removes all species not bound to the capture antibody (including analyte-label antibody complexes) and leads to a lower-than-expected signal during detection.
Note that in this case the micropatterns next to the cell give some contrast in the deflection image; we attribute the signal to shedded and crosslinked protein clusters, which are specifically bound to the capture antibody spots via GFP.
The purified EEHV-gB antigen was diluted in PBS containing 0.1 % Triton-X to a concentration of 750 ng/well and bound to the capture antibody for 1 h at 37 °C.
The sample is mixed with a detection cocktail consisting of a) capture beads coated with antibodies specific for the target(s) of interest and b) detection antibodies labeled with a fluorescent tag, which will be bound to the capture bead in the presence of the corresponding antigen.
Similar(52)
Figitumumab bound to the capturing receptor was then detected using horseradish peroxidase-conjugated mouse anti-human IgG2.
A secondary biotinylated detection antibody that bound to the cytokine captured on the bead was incubated with the samples.
The red lines on detection pad were generated when the gold nanoparticles conjugated antibody bound to the fluorescein labelled amplicons, and the capture agents bound to their specific hapten on the other 5′ end of the double-stranded amplicon.
The captured DNA bound to the beads was subjected to LM-PCR as outlined in the Nimbelgen SeqCap EZ protocol except that the number of cycles was reduced to 10.
A conformational intermediate, having an additional Mg II) bound to the cleavage-site phosphate, was captured by freeze-trapping the RNA at an active pH prior to cleavage.
More suggestions(18)
related to the capture
bind to the capture
bound to the corpse
bound to the polymer
bound to the promoter
bound to the shale
bound to the tent
bound to the attic
bound to the chair
bound to the time
bound to the vision
bound to the network
bound to the macro-economy
bound to the ground
bound to the glass
bound to the unit
bound to the scaffold
bound to the past
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